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Capa Validation Engineer Jobs (NOW HIRING)

We are currently looking for a Validation Engineer to work for a leading Greater Los Angeles area ... Familiarity with deviation investigations, CAPA processes, and audit responses. * Basic vendor ...

The Validation Engineer oversees the aseptic process simulations (media fills), equipment ... Drive CAPA's assigned to the validation department * Generate and approve SCA Certificate of ...

The Validation Engineer oversees the aseptic process simulations (media fills), equipment ... Drive CAPA's assigned to the validation department * Generate and approve SCA Certificate of ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

IL ยท On-site

Manufacturing Validation Engineer Location: Lake County, IL Duration: Long Term Position Overview ... Investigate deviations, support CAPA implementation, and participate in root cause analysis.

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

Support deviations, investigations, CAPA, and change control activities associated with validation projects. * Review engineering and technical documentation to ensure validation requirements are ...

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Capa Validation Engineer information

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How much do capa validation engineer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for capa validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What are popular job titles related to Capa Validation Engineer jobs?

For Capa Validation Engineer jobs, the most frequently searched job titles are:

Infographic showing various Capa Validation Engineer job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 2% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Concord, NC โ€ข On-site

Contractor

Re-posted 9 days ago


Job description

Job Title: Validation Engineer
Location: Concord, NC
Duration: Long Term

Job Summary

We are seeking a motivated and detail-oriented Validation Engineer to support validation activities within a GMP-regulated biopharmaceutical manufacturing environment. The Validation Engineer will be responsible for equipment qualification, process validation, utility validation, and cleaning validation activities to ensure compliance with FDA, cGMP, and industry standards.

The ideal candidate will collaborate with Manufacturing, Quality Assurance, Engineering, and Regulatory teams to support production operations, maintain validated systems, and ensure regulatory compliance across the facility.

Key Responsibilities

  • Develop, execute, and review validation protocols and reports including IQ, OQ, and PQ documentation
  • Support equipment qualification activities for biopharmaceutical manufacturing equipment and laboratory systems
  • Perform process validation for upstream and downstream manufacturing processes
  • Execute cleaning validation and utility qualification activities including HVAC, purified water, compressed gases, and cleanroom systems
  • Ensure compliance with FDA, cGMP, GDP, and company quality standards
  • Support computerized systems validation (CSV) activities when required
  • Participate in deviation investigations, root cause analysis, CAPA, and change control processes
  • Collaborate with cross-functional teams during equipment installation, commissioning, and technology transfer projects
  • Maintain validation lifecycle documentation including SOPs, Validation Master Plans (VMP), and risk assessments
  • Assist during internal audits and regulatory inspections by providing validation documentation and technical support
  • Identify and implement continuous improvement opportunities within validation and manufacturing processes

Required Qualifications

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, or related field
  • 3+ years of validation experience in biopharmaceutical, pharmaceutical, or regulated manufacturing industries
  • Strong understanding of cGMP, FDA regulations, and validation principles
  • Experience with IQ/OQ/PQ protocol execution and report generation
  • Knowledge of process validation, cleaning validation, and utility qualification
  • Familiarity with deviation management, CAPA, and change control systems
  • Strong technical writing and documentation skills
  • Excellent communication, analytical, and problem-solving abilities